307 related articles for article (PubMed ID: 27055195)
1. Disorders of Sex Development with Testicular Differentiation in SRY-Negative 46,XX Individuals: Clinical and Genetic Aspects.
Grinspon RP; Rey RA
Sex Dev; 2016; 10(1):1-11. PubMed ID: 27055195
[TBL] [Abstract][Full Text] [Related]
2. Testicular differentiation in 46,XX DSD: an overview of genetic causes.
Ferrari MTM; Silva ESDN; Nishi MY; Batista RL; Mendonca BB; Domenice S
Front Endocrinol (Lausanne); 2024; 15():1385901. PubMed ID: 38721146
[TBL] [Abstract][Full Text] [Related]
3. Diagnosis and management of non-CAH 46,XX disorders/differences in sex development.
Yavas Abalı Z; Guran T
Front Endocrinol (Lausanne); 2024; 15():1354759. PubMed ID: 38812815
[TBL] [Abstract][Full Text] [Related]
4. A Duplication Upstream of SOX9 Associated with
Mengen E; Kayhan G; Kocaay P; Uçaktürk SA
J Clin Res Pediatr Endocrinol; 2020 Sep; 12(3):308-314. PubMed ID: 31476840
[TBL] [Abstract][Full Text] [Related]
5. Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD.
Seeherunvong T; Ukarapong S; McElreavey K; Berkovitz GD; Perera EM
J Pediatr Endocrinol Metab; 2012; 25(1-2):121-3. PubMed ID: 22570960
[TBL] [Abstract][Full Text] [Related]
6. Coexistence of Trisomy 13 and SRY (-) XX Ovotesticular Disorder of Sex Development.
Ürel Demir G; Doğan ÖA; Şimşek Kiper PÖ; Utine GE; Boduroğlu K; Gucer S; Alikaşifoğlu M
Fetal Pediatr Pathol; 2017 Dec; 36(6):445-451. PubMed ID: 29220612
[TBL] [Abstract][Full Text] [Related]
7.
Richardson N; Gillot I; Gregoire EP; Youssef SA; de Rooij D; de Bruin A; De Cian MC; Chaboissier MC
Elife; 2020 May; 9():. PubMed ID: 32450947
[TBL] [Abstract][Full Text] [Related]
8. In Tandem Intragenic Duplication of Doublesex and Mab-3-Related Transcription Factor 1 (
Bertini V; Baldinotti F; Parma P; Tyutyusheva N; Sepich M; Bertolucci G; Rosano C; Caligo MA; Peroni D; Valetto A; Bertelloni S
Genes (Basel); 2023 Nov; 14(11):. PubMed ID: 38003010
[TBL] [Abstract][Full Text] [Related]
9. Are NR5A1 Variations a Frequent Cause of 46,XX Ovotesticular Disorders of Sex Development? Analysis from a Single Center and Systematic Review.
Barros BA; Guaragna MS; Fabbri-Scallet H; Palandi de Mello M; Guerra-Júnior G; Maciel-Guerra AT
Sex Dev; 2022; 16(4):242-251. PubMed ID: 36657429
[TBL] [Abstract][Full Text] [Related]
10. NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development.
Baetens D; Stoop H; Peelman F; Todeschini AL; Rosseel T; Coppieters F; Veitia RA; Looijenga LH; De Baere E; Cools M
Genet Med; 2017 Apr; 19(4):367-376. PubMed ID: 27490115
[TBL] [Abstract][Full Text] [Related]
11. A duplication upstream of SOX9 was not positively correlated with the SRY‑negative 46,XX testicular disorder of sex development: A case report and literature review.
Xia XY; Zhang C; Li TF; Wu QY; Li N; Li WW; Cui YX; Li XJ; Shi YC
Mol Med Rep; 2015 Oct; 12(4):5659-64. PubMed ID: 26260363
[TBL] [Abstract][Full Text] [Related]
12. Duplication of SOX3 in an SRY-negative 46,XX male with prostatic utricle: case report and literature review.
Wei J; Liu C; Zhang M; Liu S; Fu J; Lin P
BMC Med Genomics; 2022 Sep; 15(1):188. PubMed ID: 36064700
[TBL] [Abstract][Full Text] [Related]
13. XX Maleness and XX true hermaphroditism in SRY-negative monozygotic twins: additional evidence for a common origin.
Maciel-Guerra AT; de Mello MP; Coeli FB; Ribeiro ML; Miranda ML; Marques-de-Faria AP; Baptista MT; Moraes SG; Guerra-Júnior G
J Clin Endocrinol Metab; 2008 Feb; 93(2):339-43. PubMed ID: 18056774
[TBL] [Abstract][Full Text] [Related]
14. SRY-negative 46,XX testicular/ovotesticular DSD: Long-term outcomes and early blockade of gonadotropic axis.
Lambert S; Peycelon M; Samara-Boustani D; Hyon C; Dumeige L; Peuchmaur M; Fiot E; Léger J; Simon D; Paye-Jaouen A; Bouligand J; Siffroi JP; Carel JC; McElreavey K; El Ghoneimi A; Brachet C; Bouvattier C; Martinerie L
Clin Endocrinol (Oxf); 2021 Apr; 94(4):667-676. PubMed ID: 33296530
[TBL] [Abstract][Full Text] [Related]
15. Extended pedigree with multiple cases of XX sex reversal in the absence of SRY and of a mutation at the SOX9 locus.
Temel SG; Gulten T; Yakut T; Saglam H; Kilic N; Bausch E; Jin WJ; Leipoldt M; Scherer G
Sex Dev; 2007; 1(1):24-34. PubMed ID: 18391513
[TBL] [Abstract][Full Text] [Related]
16. A Follow-Up from Infancy to Puberty in a Japanese Male with SRY-Negative 46,XX Testicular Disorder of Sex Development Carrying a p.Arg92Trp Mutation in NR5A1.
Saito-Hakoda A; Kanno J; Suzuki D; Kawashima S; Kamimura M; Hirano K; Sakai K; Igarashi M; Fukami M; Fujiwara I
Sex Dev; 2019; 13(2):60-66. PubMed ID: 30739115
[TBL] [Abstract][Full Text] [Related]
17. Sex determination and disorders of sex development according to the revised nomenclature and classification in 46,XX individuals.
Kousta E; Papathanasiou A; Skordis N
Hormones (Athens); 2010; 9(3):218-131. PubMed ID: 20688619
[TBL] [Abstract][Full Text] [Related]
18. A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex development.
Bashamboo A; Donohoue PA; Vilain E; Rojo S; Calvel P; Seneviratne SN; Buonocore F; Barseghyan H; Bingham N; Rosenfeld JA; Mulukutla SN; Jain M; Burrage L; Dhar S; Balasubramanyam A; Lee B; ; Dumargne MC; Eozenou C; Suntharalingham JP; de Silva K; Lin L; Bignon-Topalovic J; Poulat F; Lagos CF; McElreavey K; Achermann JC
Hum Mol Genet; 2016 Aug; 25(16):3446-3453. PubMed ID: 27378692
[TBL] [Abstract][Full Text] [Related]
19. Disorders of sexual development and associated changes in the pituitary-gonadal axis in dogs.
Buijtels JJ; de Gier J; Kooistra HS; Grinwis GC; Naan EC; Zijlstra C; Okkens AC
Theriogenology; 2012 Oct; 78(7):1618-26. PubMed ID: 22980090
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
